JPH0345780A - Chemical finish of silk fiber product - Google Patents
Chemical finish of silk fiber productInfo
- Publication number
- JPH0345780A JPH0345780A JP18123289A JP18123289A JPH0345780A JP H0345780 A JPH0345780 A JP H0345780A JP 18123289 A JP18123289 A JP 18123289A JP 18123289 A JP18123289 A JP 18123289A JP H0345780 A JPH0345780 A JP H0345780A
- Authority
- JP
- Japan
- Prior art keywords
- silk fiber
- epoxy compound
- silk
- catalyst
- metal salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 24
- 239000000126 substance Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 30
- 239000004593 Epoxy Substances 0.000 claims abstract description 28
- 239000003054 catalyst Substances 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 8
- 238000001035 drying Methods 0.000 claims abstract description 7
- 229910052751 metal Chemical class 0.000 claims abstract description 6
- 239000002184 metal Chemical class 0.000 claims abstract description 6
- 230000007935 neutral effect Effects 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 27
- 239000004744 fabric Substances 0.000 abstract description 17
- 239000000243 solution Substances 0.000 abstract description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 6
- 150000005846 sugar alcohols Polymers 0.000 abstract description 5
- 239000007864 aqueous solution Substances 0.000 abstract description 2
- 230000006866 deterioration Effects 0.000 abstract description 2
- 159000000011 group IA salts Chemical class 0.000 abstract description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 abstract 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000010025 steaming Methods 0.000 description 6
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 5
- 239000004753 textile Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- ZQXCQTAELHSNAT-UHFFFAOYSA-N 1-chloro-3-nitro-5-(trifluoromethyl)benzene Chemical compound [O-][N+](=O)C1=CC(Cl)=CC(C(F)(F)F)=C1 ZQXCQTAELHSNAT-UHFFFAOYSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
- HDPLHDGYGLENEI-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COC(C)COCC1CO1 HDPLHDGYGLENEI-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229910001323 Li2O2 Inorganic materials 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、絹繊維製品をエポキシ化合物を用いて化学的
に改質する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for chemically modifying silk fiber products using an epoxy compound.
(従来の技術)
エポキシ化合物による絹繊維製品の改質法としては、苛
性アルカリなどの強アルカリ性物質、または四塩化編、
三ふっ化はう素などの強酸性′+!IJ質を触媒とする
方法が公知であるが、この加工法は繊維の劣化を伴なう
ものであった。また温和な触媒として有機アミンを使用
する方法(特公昭38−25198) もあるが、こ
の方法では、充分な加工効果を得ることができなかった
。(Prior art) As a method for modifying silk fiber products using epoxy compounds, strong alkaline substances such as caustic alkali, or tetrachloride,
Strong acids such as borosilicate trifluoride! A method using IJ quality as a catalyst is known, but this processing method is accompanied by deterioration of the fibers. There is also a method (Japanese Patent Publication No. 38-25198) in which an organic amine is used as a mild catalyst, but this method does not provide sufficient processing effects.
そこで、これらの改良法として、二相法と呼ばれる有機
溶剤系加工法(特公昭52−38131 )が出現した
が、この方法は、第1工程で触媒水溶液を繊維に含浸さ
せ、第2工程で有機溶剤相としてエポキシ化合物を高温
で反応させるもので、作業性が悪く、実用化を阻む多く
の欠点があった。Therefore, as an improvement method for these, an organic solvent-based processing method called the two-phase method (Japanese Patent Publication No. 52-38131) has emerged, but this method involves impregnating the fibers with an aqueous catalyst solution in the first step, and then impregnating the fibers in the second step. This method involves reacting an epoxy compound as an organic solvent phase at high temperatures, resulting in poor workability and many drawbacks that hinder its practical application.
この改善策として水性相内で反応を進める方法も提案さ
れているが、それに使用されるエポキシ化合物は、水溶
性の単官能性エポキシ化合物や、多価アルコールのジグ
リシジルエーテル物であり、触媒を処理浴に共存させて
高温反応させるものであり、この方法では溶液内でエポ
キシ化合物の樹脂化が進み、繊維に化合物が効率よく反
応しないという欠点があった。A method of proceeding with the reaction in the aqueous phase has been proposed as a method to improve this problem, but the epoxy compounds used for this are water-soluble monofunctional epoxy compounds and diglycidyl ethers of polyhydric alcohols, and the epoxy compounds used for this are water-soluble monofunctional epoxy compounds and diglycidyl ethers of polyhydric alcohols, and the epoxy compounds used for this method are water-soluble monofunctional epoxy compounds and diglycidyl ethers of polyhydric alcohols. The epoxy compound is allowed to coexist with the treatment bath and undergoes a high-temperature reaction, and this method has the disadvantage that the epoxy compound progresses to become a resin within the solution, and the compound does not react efficiently with the fibers.
更に、エポキシ化合物の有機溶剤/水混合液や水分散液
を繊維品に塗布あるいは噴射してマイクロ波照射を行う
方法(特開昭6O−252771)も知られているが、
これも前段において触媒水溶液で前処理をしておく必要
があり、処理が二段に跨がるため非能率であり、かつ均
整な処理をし難いなどの欠点があった。Furthermore, there is also known a method of coating or spraying an organic solvent/water mixture or water dispersion of an epoxy compound onto a textile product and irradiating it with microwaves (Japanese Patent Laid-Open No. 6O-252771).
This method also requires pretreatment with an aqueous catalyst solution in the first stage, and has drawbacks such as inefficiency since the treatment spans two stages, and difficulty in uniformly performing the treatment.
このような従来法の欠点を解消し、簡便でかつ既存の設
備で処理が実施できる方法として、本出願人は、コール
ドバッチ法を利用した一段処理法を開発し、特許出願し
た(特開昭64−20379号及び特開昭64−203
80号)が、この方法では、反応時間に8〜48時間を
要し、作業能率の点で問題があった。In order to overcome these drawbacks of the conventional method and to be able to carry out the treatment simply and with existing equipment, the applicant has developed a one-stage treatment method using a cold batch method and has filed a patent application (Japanese Patent Application Laid-Open No. No. 64-20379 and JP-A No. 64-203
No. 80), however, this method required a reaction time of 8 to 48 hours and had a problem in working efficiency.
(発明が解決しようとする課題)
本発明は、絹繊維製品に、短時間で均一にエポキシ化合
物を反応させ、耐摩耗性や寸法安定性等を効率よく付与
する方法を提供することを課題とする。(Problems to be Solved by the Invention) An object of the present invention is to provide a method for efficiently imparting wear resistance, dimensional stability, etc. to silk fiber products by uniformly reacting an epoxy compound in a short time. do.
(課題を解決するための手段)
本発明では多官能性エポキシ化合物と金属塩触媒を併合
する水性処理液を絹繊維製品に付着させた後、乾燥する
ことなく蒸熱処理することにより、上記課題を解決した
。(Means for Solving the Problems) The present invention solves the above problems by applying an aqueous treatment liquid that combines a polyfunctional epoxy compound and a metal salt catalyst to a silk fiber product, and then subjecting it to a steam treatment without drying. Settled.
すなわち、本発明は触媒を含んだエポキシ化合物の水性
処理液を、絹繊維に付着させた後、その反応固着に蒸熱
処理を利用するものであり、従来の溶液内反応の如き無
駄な反応が生ずることなく、エポキシ化合物を100%
近くを有効に反応固着できる。また、処理層の付着も一
段工程で効率よ〈実施でき、品質管理が容易である。That is, the present invention utilizes steaming treatment for reaction fixation after adhering an aqueous treatment solution of an epoxy compound containing a catalyst to silk fibers, which avoids wasteful reactions like conventional reactions in solution. 100% epoxy compound without any
Can effectively react and fix nearby areas. Furthermore, the attachment of the treatment layer can be carried out efficiently in a single step, and quality control is easy.
本発明に用いる多官能性エポキシ化合物としては、多価
アルコールのポリグリシジルエーテルが適当であり、例
えばエチレングリコール・ジグリシジルエーテル、ポリ
エチレングリコール・ジグリシジルエーテル、プロピレ
ングリコール・ジグリシジルエーテル、ポリプロピレン
グリコール・ジグリシジルエーテル、グリセロールジグ
リシジルエーテル、ソルビトール・ポリグリシジルエー
テル、還元マルトース・ポリグリシジルエーテル等であ
る。またジカルボン酸ジグリシジールエステル類、例え
ばコハク酸やアジピン類のジグリシジルエーテル等、さ
らには含窒素へテロ還エポキシ化合物も有効に用いるこ
とができる。これらは、単独で使用されても、2種以上
併用されてもよい。Suitable polyfunctional epoxy compounds used in the present invention include polyglycidyl ethers of polyhydric alcohols, such as ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, and polypropylene glycol diglycidyl ether. These include glycidyl ether, glycerol diglycidyl ether, sorbitol polyglycidyl ether, and reduced maltose polyglycidyl ether. In addition, dicarboxylic acid diglycidyl esters, such as diglycidyl ethers of succinic acid and adipine, and nitrogen-containing heterocyclic epoxy compounds can also be effectively used. These may be used alone or in combination of two or more.
次に触媒としては、例えばNas K SL1% Ca
、Baを陽イオン成分とする中性塩および弱アルカリ性
塩を用いるが、具体的にはチオ硫酸塩、チオシアン酸塩
、塩化物、ヨウ化物、臭化物、炭酸塩、りん酸塩、酢酸
塩等が有用である。これ等触媒はエポキシ化合物の20
〜100重量%の範囲内で用いるのが望ましい。Next, as a catalyst, for example, Nas K SL1% Ca
, neutral salts and weak alkaline salts containing Ba as a cationic component are used, specifically thiosulfates, thiocyanates, chlorides, iodides, bromides, carbonates, phosphates, acetates, etc. Useful. These catalysts are 20% of epoxy compounds.
It is desirable to use it within the range of 100% by weight.
本発明において使用する処理液は、基本的にはエポキシ
化合物と金属塩触媒を水中に併合するものであって、必
要に応して、エポキシ化合物の溶解または分散補助剤と
して、低級アルコールや界面活性剤等を少量含むもので
ある。そのl夜の状態は補助剤の種類や添加量により、
水溶l夜または水性エマルジヨンいずれかの状態をとる
。The treatment liquid used in the present invention is basically one in which an epoxy compound and a metal salt catalyst are combined in water. It contains small amounts of agents, etc. The nighttime condition depends on the type and amount of adjuvant used.
It takes the form of either an aqueous solution or an aqueous emulsion.
上記処理液を絹織物又は編物等に付与するには、通常2
〜3本の絞りロールを備えたパディング機によって行い
、処理液の被処理繊維に対する付与量を50〜200重
量%の範囲に調節するのがよい。In order to apply the above-mentioned treatment liquid to silk fabrics or knitted fabrics, it is usually necessary to
It is preferable to use a padding machine equipped with ~3 squeezing rolls, and adjust the amount of treatment liquid applied to the fibers to be treated within a range of 50 to 200% by weight.
その他の繊維製品、例えば糸等の処理は、処理液を含浸
させ、遠心機等で脱液するのがよい。When treating other textile products, such as threads, it is preferable to impregnate them with a treatment liquid and remove the liquid using a centrifuge or the like.
本発明では、処理液を飽充した繊維製品を、水分を保持
したまま加熱するものであり、乾燥することなく蒸熱処
理する。In the present invention, a textile product filled with a treatment liquid is heated while retaining moisture, and is steam-treated without drying.
この工程は、通常の繊維製品加工分野において、パッド
・スチーム法として知られるものであり、既存の設備で
十分対応できる。従って、本発明の実用化は極めて容易
となる。This process is known as the pad steam method in the field of ordinary textile processing, and can be adequately handled with existing equipment. Therefore, practical application of the present invention becomes extremely easy.
渾然処理は、通常、飽和水蒸気で満たされた90〜10
0℃の室内中に2〜60分間、処理品を置くことで目的
を達し得る。常圧型の蒸熱機であれば、15〜30分の
スチーミングで十分である。処理品の水分の蒸発を伴な
う過熱薫気の使用はむしろ好ましくない。The aeration process is usually carried out using a 90 to 10
This can be accomplished by placing the treated product in a room at 0° C. for 2 to 60 minutes. If a normal pressure steamer is used, steaming for 15 to 30 minutes is sufficient. It is rather undesirable to use superheated fumes, which evaporates water from the treated product.
なお、ip中マイクロ波を照射することは、蒸熱時間の
短縮に有効で、2〜5分間のごく短時間の蒸熱で、エポ
キシ化合物の固着を高度の効率をもって完了させること
ができる。Note that irradiation with microwaves during IP is effective in shortening the steaming time, and fixation of the epoxy compound can be completed with a high degree of efficiency by steaming for a very short time of 2 to 5 minutes.
本発明では、このような蒸熱処理の採用により、絹繊維
製品にエポキシ化合物を短時間で均一に効率よく反応固
着できるものであり、連続式の蒸熱機の採用と、処理液
の一段パソディング法とが相俟て、生産性が著しく高め
られ、しかも加工班のない均一な品質の製品の生産を安
定して可能とする。In the present invention, by adopting such a steaming treatment, an epoxy compound can be reacted and fixed to silk fiber products uniformly and efficiently in a short time. Together, this significantly increases productivity and makes it possible to stably produce products of uniform quality without the need for processing teams.
なお、本発明において絹繊維製品とは、絹繊維を含む製
品を意味するものであり、絹繊維単独からなる編織布、
糸等だけでなく、絹mMと他の繊維の混紡品、交織又は
交編布をも含む。Note that in the present invention, the term "silk fiber product" refers to a product containing silk fibers, and includes knitted and woven fabrics made solely of silk fibers,
It includes not only threads but also blends of silk mm and other fibers, interwoven or interwoven fabrics.
以下、実施例により具体的に説明する。Hereinafter, this will be explained in detail using examples.
実施例1
t#練済みの絹論子ちりめん(14目付) 33.9g
rを、下記の水性処理液中に浸漬した後、マングルで脱
液した (絞り率120%)
イソプロパツール 120
チオシアン酸ナトリウム 80〃水
700この処理布を
乾燥することなく、飽和水蒸気で満たされた98℃の蒸
熱室内に20分間入れて蒸熱を行い、次いでソーピング
、水洗、乾燥をして37.8grの処理布を得た。この
場合の加工増量率は10.3%、反応率は96%にも及
んだ。Example 1 T# Kneaded Silk Ronshi Chirimen (14 stitches) 33.9g
r was immersed in the following aqueous treatment solution, and then drained with a mangle (squeezing ratio 120%) Isopropatol 120 Sodium thiocyanate 80 Water
700 This treated cloth was steamed without drying by placing it in a 98° C. steaming chamber filled with saturated steam for 20 minutes, followed by soaping, washing, and drying to obtain a treated cloth weighing 37.8 gr. In this case, the processing weight increase rate was 10.3% and the reaction rate was as high as 96%.
ただし
増量率=(増分/処理前布型1) X100効率 −(
増分/付着した樹脂分)X100増分 −処理前後の布
の重量増加分
(圧)付着した樹脂分とは、処理布のピックアップした
液中に含まれるエポキシ化合物の重量である。However, increase rate = (increment/pre-treatment fabric type 1) X100 efficiency - (
Increment/adhered resin content) x 100 increment - weight increase (pressure) of the cloth before and after treatment The adhered resin content is the weight of the epoxy compound contained in the liquid picked up by the treated cloth.
この処理布の性能を第1表に示す。The performance of this treated fabric is shown in Table 1.
第1表
(注)
吸湿=20℃、65%H,24Hr!jilrW防しわ
度; JIS Li2O2針金法収lit : JI
S L1042 [1法スレ: JIS学振型摩擦
試験機、500.荷重、ナイロン布200回摩擦、肉眼
観察による官能検査
実施例2
実施例1と同し絹ra物34.1grを、下記の水性処
理液中に浸漬した後、ウェア トビツクアップ120%
にてマングル脱液した。Table 1 (Note) Moisture absorption = 20℃, 65%H, 24Hr! jilrW wrinkle resistance; JIS Li2O2 wire method collection lit: JI
SL1042 [1 method thread: JIS Gakushin type friction tester, 500. Sensory test using load, rubbing nylon cloth 200 times, and visual observation Example 2 After immersing 34.1g of the same silk material as in Example 1 in the following aqueous treatment solution, the wear was lifted up by 120%.
The mangle was dehydrated.
非イオン系界面活性剤 15
チオシアン酸ナトリウム 80
水
05
この処理布を実施例1と同様蒸熱し、後処理乾燥すると
、最終布ff1lは38.1grとなった。Nonionic surfactant 15 Sodium thiocyanate 80 Water 05 This treated cloth was steamed in the same manner as in Example 1, and after-treatment and drying, the final cloth ff1l had a weight of 38.1 gr.
このときの増量率は11.7%、効率は98%であった
。この処理布の性能を洗濯収縮率でみると第2表の通り
である。At this time, the increase rate was 11.7% and the efficiency was 98%. Table 2 shows the performance of this treated fabric in terms of washing shrinkage rate.
第2表
実施例3
実施例2と同様の絹織物3.41grを実施例1と同し
処方の液に浸漬し、マングル脱′/&(絞り率120%
)した、このものを家庭用電子レンジ (高周波出力5
00W)内に置き、水蒸気を導入して3分間加熱を行っ
た。この際の増量率13.2%、効率は見掛計算のため
100を越え110%にもなった。Table 2 Example 3 3.41 gr of the same silk fabric as in Example 2 was immersed in a liquid with the same formulation as in Example 1, and demangled '/& (squeezing rate 120%).
), this product can be used in a home microwave oven (high frequency output 5
00W), water vapor was introduced, and heating was performed for 3 minutes. At this time, the increase rate was 13.2%, and the efficiency exceeded 100 and reached 110% due to the apparent calculation.
(発明の効果)
本発明の方法では、特別な装置を用いることなく既存の
設備で、−工程で必要な薬液を絹繊維品に付与し、引き
続き当該品をN熱することにより、エポキシ化合物を絹
繊維に安定して反応固着させ得ることができる。従って
、生産性が非常に高く、しかも均整度のよい処理布を得
ることができる。(Effects of the Invention) In the method of the present invention, an epoxy compound is produced by applying the chemical solution required in the step to a silk fiber product and subsequently heating the product with N using existing equipment without using any special equipment. It can be stably reacted and fixed to silk fibers. Therefore, it is possible to obtain a treated cloth with very high productivity and good uniformity.
更に、本発明の方法で得られる製品は良好な寸法安定性
と耐摩耗性に優れるもので、家庭洗濯の可能な絹繊維製
品の製造に貢献するものとなる。Furthermore, the product obtained by the method of the present invention has good dimensional stability and excellent abrasion resistance, and will contribute to the production of silk fiber products that can be washed at home.
Claims (1)
弱アルカリ性の金属塩とを併合する水性処理液を、絹繊
維製品に付着させ、乾燥することなく蒸熱処理し、エポ
キシ化合物を絹繊維に固着させることを特徴とする絹繊
維製品の化学的加工方法。An aqueous treatment solution that combines a polyfunctional epoxy compound and a neutral or weakly alkaline metal salt as a catalyst is applied to a silk fiber product, and then steamed without drying to fix the epoxy compound to the silk fiber. A method for chemically processing silk fiber products.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18123289A JPH0345780A (en) | 1989-07-12 | 1989-07-12 | Chemical finish of silk fiber product |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18123289A JPH0345780A (en) | 1989-07-12 | 1989-07-12 | Chemical finish of silk fiber product |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0345780A true JPH0345780A (en) | 1991-02-27 |
Family
ID=16097114
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18123289A Pending JPH0345780A (en) | 1989-07-12 | 1989-07-12 | Chemical finish of silk fiber product |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0345780A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994002675A1 (en) * | 1992-07-17 | 1994-02-03 | Tuyaku Co., Ltd. | Method of stabilizing hygral expansion of protein fiber product |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6181369A (en) * | 1984-09-27 | 1986-04-24 | フジテツク株式会社 | Method of controlling group of elevator |
JPS6327471A (en) * | 1986-07-21 | 1988-02-05 | Yamanouchi Pharmaceut Co Ltd | Production of optically active benzenesulfonamide derivative |
JPS6426784A (en) * | 1987-04-28 | 1989-01-30 | Kanebo Ltd | Method for processing silk fiber |
-
1989
- 1989-07-12 JP JP18123289A patent/JPH0345780A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6181369A (en) * | 1984-09-27 | 1986-04-24 | フジテツク株式会社 | Method of controlling group of elevator |
JPS6327471A (en) * | 1986-07-21 | 1988-02-05 | Yamanouchi Pharmaceut Co Ltd | Production of optically active benzenesulfonamide derivative |
JPS6426784A (en) * | 1987-04-28 | 1989-01-30 | Kanebo Ltd | Method for processing silk fiber |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994002675A1 (en) * | 1992-07-17 | 1994-02-03 | Tuyaku Co., Ltd. | Method of stabilizing hygral expansion of protein fiber product |
US5494487A (en) * | 1992-07-17 | 1996-02-27 | Tuyaku Co., Ltd. | Method for stabilizing the hygral expansion behavior of protein fiber products |
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